A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549333



Internal ID20922495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45078964..45095318hg38UCSC Ensembl
chr21:46498879..46515233hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816355
hg1916355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073352
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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